Classification Report Template

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Price: $150

This template provides a detailed outline of the classification rules for your medical device in accordance with Annex VIII of Medical Device Regulation (EU) 2017/745 (MDR). This template delineates the justification for the applicability or non-applicability of classification based on the device’s intended use and inherent risk.

This template is written by highly experienced professionals for all medical device companies. Click below to get a preview of this template.